Background: The destructive insect pest Agrotis ipsilon (Hufnagel) (Lepidoptera: Noctuidae) is a polyphagous species targeting many economically important plants. The extensive and arbitrary use of insecticides has resulted in the build-up of insecticide resistance and pesticide residues accumulating in food. Therefore, it is becoming evident that alternative pest management tools are needed to reduce risks to humans, the environment, and non-target organisms, and at the same time, they should be used in field application at the lowest cost. Methods: In view of this objective, the present study demonstrates the toxicity of lemongrass (Cymbopogon citratus (DC.) Stapf) essential oil (EO), against the black cutworm A. ipsilon under controlled laboratory conditions in terms of measuring the activity of peroxidase and detoxification enzymes. The chemical components of the EO were analyzed using GC–MS. Results: The results show that after 96 h post treatment, the LC15 and LC50 values were 427.67 and 2623.06 mg/L, respectively, of C. citratus EO on second-instar larvae of A. ipsilon. A slight significance in elongation of the larval duration with LC15 and LC50 value was found with control. By GC–MS analysis, the main compounds identified in the EO were α-citral and β-citral with percentages of 35.91%, and 35%, respectively. The oxidative stress indicates a significant increase in CAT and lipid peroxidase enzyme activity after 96 h post treatment at the LC15 and LC50. Conversely, the detoxification enzyme activity shows an inhibition of CarE and GST enzymes of larvae exposed to LC15 and LC50 values in response to C. citratus EO. Conclusions: The present data show that lemongrass EO has insecticidal activity against the black cutworm, A. ipsilon.

Insecticide resistance is a significant problem in insect management that can result from several processes including target-site change and increased activity of detoxifying enzymes. Spodoptera littoralis is one of the most resistant insect pests. For more effective insect management, alternatives to synthetic pesticides are encouraged. One of these alternatives is essential oils (EOs). Cymbopogon citratus EO and its main constituent citral were, therefore, considered in this study. The results revealed that C. citratus EO and citral exhibited significant larvicidal activity against S. littoralis, and the former was insignificantly more toxic than the latter. Additionally, treatments significantly affected the activity of detoxification enzymes. Cytochrome P-450 and glutathione-S-transferase were inhibited, while carboxylesterases, a-esterase and β-esterase, were induced. The molecular docking study indicated that citral bonded with the amino acids cysteine (CYS 345) and histidine (HIS 343) of cytochrome P-450. This result suggests that interaction with cytochrome P-450 enzyme is one key mechanism by which C. citratus EO and citral act in S. littoralis. The results of our study are hoped to contribute to a better understanding of the mechanism of action of essential oils at the biochemical and molecular levels and provide safer and more efficient pest management solutions for S. littoralis.

Background: Spodoptera littoralis (Boisd.) is a prominent agricultural insect pest that has developed resistance to a variety of insecticide classes. In this study, the resistance of three field strains of S. littoralis, collected over three consecutive seasons (2018 to 2020) from three Egyptian Governorates (El-Fayoum, Behera and Kafr El-Shiekh), to six insecticides was monitored. Methods: Laboratory bioassays were carried out using the leaf-dipping method to examine the susceptibility of the laboratory and field strains to the tested insecticides. Activities of detoxification enzymes were determined in an attempt to identify resistance mechanisms. Results: The results showed that LC50 values of the field strains ranged from 0.0089 to 132.24 mg/L, and the corresponding resistance ratio (RR) ranged from 0.17 to 4.13-fold compared with the susceptible strain. Notably, low resistance developed to spinosad in all field strains, and very low resistance developed to alpha-cypermethrin and chlorpyrifos. On the other hand, no resistance developed to methomyl, hexaflumeron or Bacillus thuringiensis. The determination of detoxification enzymes, including carboxylesterases (α- and β-esterase), mixed function oxidase (MFO) and glutathione-S-transferase (GST), or the target site of acetylcholinesterase (AChE), revealed that the three field strains had significantly different activity levels compared with the susceptible strain. Conclusion: Our findings, along with other tactics, are expected to help with the resistance management of S. littoralis in Egypt.

Cypermethrin, esfenvalerate, chlorpyrifos and Bacillus thuringiensis, Kurs. were tested against the cotton leaf worm, Spodoptera littoralis (Boisd.) treated as 4 th instar larvae. In addition, LC 50 , s of tested compounds were applied on S. littoralis larvae to investigate the ultra structural changes in the integument, muscle, fat body and mid gut of alive and dead larvae. Meanwhile, the nerve cord sections were investigated for alive larvae only. All investigations were done by light and electronic microscopes.Cypermethrin was the most potent compounds against S. littoralis larvae, followed by esfenvalerate, chlorpyrifos and then B. thuringiensis that had the least toxicity on the cotton leaf worm compared to other tested compounds.Ultra structural investigations showed that cypermethrin caused thickening of outer cuticle fibrous layer in the integument of S. littoralis larvae. Also, hypodermis layer had swelling at the same treatment and necrosis in other treatments. In addition, all the treatments caused appearance of fissure and breaking down of muscles into small parts. While, all tested compounds except B. thuringiensis caused swelling in the integuments of dead larvae compared to control. On the other hand, B. thuringiensis caused drastically necrosis in the integument and hypodermis layers of dead larvae. All the compounds caused a noticeable destruction on the fat body cells as well as vacuolization and destruction the fat body membranous sheath. Many deleterious effects in the mid gut of S. littoralis as destruction of columnar or hyperphesia cells lining mid gut, losses of brush border with increase of goblet cells. Mid gut of died larvae had the highly destruction as affected by cypermethrin treatment. Meanwhile, other treatments caused shrinking in mid gut parts and necrosis in another parts. Neurosecretory cells of S. littoralis larval nerve cord had shrunk and dwarfed in cypermethrin, chlorpyrifos and B. thuringiensis, while; it had swelling in esfenvalerate treatment. Also, nucleus and nerve cells were disappeared partly in the most treatment compared to control.

Pesticide application can have an adverse effect on pollinator honey bees, Apis mellifera L., ranging from mortality to sublethal effects. Therefore, it is necessary to understand any potential effects of pesticides. The present study reports the acute toxicity and adverse effects of sulfoxaflor insecticide on the biochemical activity and histological changes on A. mellifera. The results showed that after 48 h post-treatment, the LD25 and LD50 values were 0.078 and 0.162 µg/bee, respectively, of sulfoxaflor on A. mellifera. The detoxification enzyme activity shows an increase of glutathione-S-transferase (GST) enzyme on A. mellifera in response to sulfoxaflor at LD50 value. Conversely, no significant differences were found in mixed-function oxidation (MFO) activity. In addition, after 4 h of sulfoxaflor exposure, the brains of treated bees showed nuclear pyknosis and degeneration in some cells, which evolved to mushroom shaped tissue losses, mainly neurons replaced by vacuoles after 48 h. There was a slight effect on secretory vesicles in the hypopharyngeal gland after 4 h of exposure. After 48 h, the vacuolar cytoplasm and basophilic pyknotic nuclei were lost in the atrophied acini. After exposure to sulfoxaflor, the midgut of A. mellifera workers showed histological changes in epithelial cells. These findings of the present study showed that sulfoxaflor could have an adverse effect on A. mellifera.